CH654019A5 - Reaktive disazo-verbindung. - Google Patents
Reaktive disazo-verbindung. Download PDFInfo
- Publication number
- CH654019A5 CH654019A5 CH1861/83A CH186183A CH654019A5 CH 654019 A5 CH654019 A5 CH 654019A5 CH 1861/83 A CH1861/83 A CH 1861/83A CH 186183 A CH186183 A CH 186183A CH 654019 A5 CH654019 A5 CH 654019A5
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- cooh
- phenylene
- water
- hydrogen
- Prior art date
Links
- LCZPIYCNOWJWPQ-UHFFFAOYSA-I disodium;chromium(3+);1-[(2-oxidonaphthalen-1-yl)diazenyl]-4-sulfonaphthalen-2-olate;3-oxido-4-[(2-oxidonaphthalen-1-yl)diazenyl]naphthalene-1-sulfonate Chemical compound [Na+].[Na+].[Cr+3].C12=CC=CC=C2C(S(=O)(=O)O)=CC([O-])=C1N=NC1=C([O-])C=CC2=CC=CC=C12.C1=CC=C2C(N=NC3=C4C=CC=CC4=CC=C3[O-])=C([O-])C=C(S([O-])(=O)=O)C2=C1 LCZPIYCNOWJWPQ-UHFFFAOYSA-I 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 239000000975 dye Substances 0.000 claims description 23
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 20
- -1 disazo compound Chemical class 0.000 claims description 16
- 239000004744 fabric Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 11
- 238000004043 dyeing Methods 0.000 claims description 10
- 239000000835 fiber Substances 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 5
- 229920003043 Cellulose fiber Polymers 0.000 claims description 4
- 150000004985 diamines Chemical class 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000010919 dye waste Substances 0.000 claims 1
- 238000007086 side reaction Methods 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 11
- 239000011230 binding agent Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229910000029 sodium carbonate Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000000980 acid dye Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 150000001989 diazonium salts Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 1
- ORLGPUVJERIKLW-UHFFFAOYSA-N 5-chlorotriazine Chemical compound ClC1=CN=NN=C1 ORLGPUVJERIKLW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- POWFTOSLLWLEBN-UHFFFAOYSA-N tetrasodium;silicate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-] POWFTOSLLWLEBN-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/043—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring containing two or more triazine rings linked together by a non-chromophoric link
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56122925A JPS5825357A (ja) | 1981-08-07 | 1981-08-07 | 反応性ジスアゾ化合物及びそれを用いるセルロ−ス系繊維の染色法 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH654019A5 true CH654019A5 (de) | 1986-01-31 |
Family
ID=14847996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH1861/83A CH654019A5 (de) | 1981-08-07 | 1982-08-06 | Reaktive disazo-verbindung. |
Country Status (5)
Country | Link |
---|---|
US (1) | US4584367A (en, 2012) |
JP (1) | JPS5825357A (en, 2012) |
CH (1) | CH654019A5 (en, 2012) |
GB (1) | GB2116991B (en, 2012) |
WO (1) | WO1983000495A1 (en, 2012) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4670341A (en) * | 1985-05-17 | 1987-06-02 | W. R. Grace & Co. | Hollow fiber |
JPH0619047B2 (ja) * | 1985-05-28 | 1994-03-16 | 三菱化成株式会社 | ジスアゾ系色素及びこれを用いる染色方法 |
DE3600527A1 (de) * | 1986-01-10 | 1987-07-16 | Fresenius Ag | Filter zur gewinnung von plasma bzw. plasmawasser, sowie verfahren zu seiner herstellung |
US5196033A (en) * | 1986-08-15 | 1993-03-23 | Imperial Chemical Industries Plc | BIS-azotriazinyl reactive dyes having an N-alkyl-phenylenediamine link for cellulose textiles |
GB8619914D0 (en) * | 1986-08-15 | 1986-09-24 | Ici Plc | Reactive dyes |
GB8828222D0 (en) * | 1988-12-02 | 1989-01-05 | Ici Plc | Reactive dyes |
US5269816A (en) * | 1988-12-02 | 1993-12-14 | Imperial Chemical Industries Plc | Process for coloring textile materials |
US5714327A (en) * | 1990-07-19 | 1998-02-03 | Kreatech Diagnostics | Platinum-containing compounds, methods for their preparation and applications thereof |
GB9016449D0 (en) * | 1990-07-26 | 1990-09-12 | Ici Plc | Anionic compounds |
DE69302039T2 (de) * | 1992-03-06 | 1996-09-12 | Zeneca Ltd | Tintenzusammensetzungen |
EP0584045B1 (de) * | 1992-08-19 | 2000-03-01 | Ciba SC Holding AG | Faserreaktive Farbstoffe, deren Herstellung und Verwendung |
GB9325454D0 (en) * | 1993-01-12 | 1994-02-16 | Zeneca Ltd | Azo compound |
US7442780B2 (en) * | 2001-05-29 | 2008-10-28 | North Carolina State University | Reactive dye compounds |
KR101036958B1 (ko) * | 2010-09-28 | 2011-05-25 | 진주현 | 셀룰로오스계 섬유의 반응성 염료 염색 시 사용되는 알칼리 고착제 조성물 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1283771A (en) * | 1969-01-16 | 1972-08-02 | Ici Ltd | New reactive disazo dyestuffs |
DE2635158C3 (de) * | 1976-08-05 | 1980-03-27 | Basf Ag, 6700 Ludwigshafen | Disazo-Reaktivf arbstoffe, Verfahren zu ihrer Herstellung und deren Verwendung zum Farben und Bedrucken von cellulosehaltigen Fasern |
JPS5857465B2 (ja) * | 1976-11-12 | 1983-12-20 | 日本化薬株式会社 | 新規反応性アゾ染料、その製法及びそれによる染色法 |
JPS5374186A (en) * | 1976-12-13 | 1978-07-01 | Mitsubishi Chem Ind | Dyeing of cellulosic fiber |
-
1981
- 1981-08-07 JP JP56122925A patent/JPS5825357A/ja active Granted
-
1982
- 1982-08-06 WO PCT/JP1982/000307 patent/WO1983000495A1/ja active Application Filing
- 1982-08-06 GB GB08308365A patent/GB2116991B/en not_active Expired
- 1982-08-06 CH CH1861/83A patent/CH654019A5/de not_active IP Right Cessation
- 1982-08-06 US US06/485,116 patent/US4584367A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0231749B2 (en, 2012) | 1990-07-16 |
JPS5825357A (ja) | 1983-02-15 |
GB2116991A (en) | 1983-10-05 |
GB8308365D0 (en) | 1983-05-05 |
WO1983000495A1 (en) | 1983-02-17 |
US4584367A (en) | 1986-04-22 |
GB2116991B (en) | 1985-01-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE3314663A1 (de) | Verfahren zum (an) faerben von cellulosefasern oder cellulosemischfasern und die dafuer verwendbaren farbstoffe | |
DE4031650C2 (de) | Farbstoffgemische und ihre Verwendung in Trichromie-Färbeprozessen | |
CH654019A5 (de) | Reaktive disazo-verbindung. | |
CH645914A5 (de) | Reaktive disazoverbindungen. | |
CH662580A5 (de) | Disazo-reaktivfarbstoffe. | |
EP0610156B1 (de) | Verfahren zum Färben oder Bedrucken von cellulosehaltigen Fasermaterialien | |
DE2658268C2 (de) | Reaktive Disazofarbstoffe mit Monochlortriazin-Reaktivgruppen, deren Herstellung und Verwendung zum Färben oder Bedrucken von Textilgut | |
DE2154942C3 (de) | faserreaktive Monoazofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zum Färben oder Bedrucken von nativen oder regenerierten Cellulosefasern, natürlichen oder synthetischen Polyamidfasern oder von Polyurethanfasern | |
DE102009045207A1 (de) | Neuer Reaktivfarbstoff mit Dialkyletherbrückengruppe | |
DE2360725C3 (de) | 09.12.72 Japan 123701-72 10.07.73 Japan 77066-73 19.07.73 Japan 82271-73 Triazinylen-bisazofarbstoffe und Verfahren zu ihrer Herstellung | |
DE69702963T2 (de) | Faserreaktive farbstoffe | |
DE1950311A1 (de) | Neue faserreaktive Farbstoffe und Faerbeverfahren unter Verwendung dieser Farbstoffe | |
EP0832940B1 (de) | Farbstoffmischungen, Verfahren zu deren Herstellung und deren Verwendung | |
DE3446053C2 (de) | Disazoverbindungen und Färbeverfahren unter Verwendung derselben | |
EP1088858B1 (de) | Reaktivfarbstoffe, enthaltend einen Formazan- und einen Monoazofarbstoffrest, Verfahren zu deren Herstellung und deren Verwendung | |
EP0857762B1 (de) | Wässrige Reaktivfarbstoff-Formulierungen sowie Verfahren zum Färben und Bedrucken von textilen Fasermaterialien | |
EP0699719B1 (de) | Azofarbstoffe, Verfahren zu deren Herstellung und deren Verwendung | |
DE3427806C2 (en, 2012) | ||
DE2706417A1 (de) | Monoazoverbindungen enthaltend einen pyrimidinrest | |
DE3248942A1 (de) | Reaktive disazoverbindung und ein verfahren zum faerben von cellulosefasern mit dieser verbindung | |
DE3331861C2 (en, 2012) | ||
DE1644377C (de) | Monoazoverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zum Färben von Textilgut | |
DE2757681A1 (de) | Phenylazopyridon-verbindung, verfahren zu deren herstellung, ihre verwendung als farbstoff und mit ihr gefaerbte fasermaterialien | |
EP0866100A2 (de) | Reaktivfarbstoffe, ihre Herstellung und Verwendung | |
AT162599B (de) | Verfahren zur Herstellung von neuen Polyazofarbstoffen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PL | Patent ceased |